Skimmia japonica - Unknown
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Internal ID UUID644004fd272c3118696026
Scientific name Skimmia japonica
Authority Thunb.
First published in Nov. Gen. Pl. : 58 (1783)

Description Top

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Synonyms Top

Scientific name Authority First published in
Skimmia fragrantissima hort. ex T.Moore Proc. Linn. Soc. London 1866-1867: vii (1867)
Skimmia fragrans Carrière Rev. Hort. (Paris) 41: 258 (1869)
Skimmia veitchii Carrière Rev. Hort. (Paris) 40: 259 (1869)
Skimmia oblata T.Moore Gard. Chron. 1864: 962 (1864)
Skimmia rugosa Makino Bot. Mag. (Tokyo) 25: 16 (1911)
Ilex skimmia Spreng. Syst. Veg. 1: 495 (1824)

Common names Top

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Language Common/alternative name
English japanese skimmia
Czech skimie japonská
Danish japansk skimmia
Persian اسکیمیا ژاپنی
Upper Sorbian japanska skimija
Japanese ミヤマシキミ
Slovak skimia japonská
Swedish vinterbär
Chinese 日本茵芋
Chinese 香茵芋

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Skimmia japonica subsp. distincte-venulosa (Hayata) T.C.Ho Endemic Sp. Res. 9(2): 41 (2007)

Varieties (abbr. var.) Top

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Name Authority First published in
Skimmia japonica var. arisanensis (Hayata) T.Yamaz. J. Jap. Bot. 68(5): 305 (1993):.
Skimmia japonica var. distincte-venulosa (Hayata) C.E.Chang Fl. Taiwan 3: 527. 1977
Skimmia japonica var. lutchuensis (Nakai) T.Yamaz. J. Jap. Bot. 68: 303 (1993)
Skimmia japonica var. orthoclada (Hayata) T.C.Ho Endemic Sp. Res. 9(2): 42. 2007 [Jan 2007]

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Name Authority First published in
Skimmia japonica f. rugosa (Yatabe) Ohwi Bull. Natl. Sci. Mus. 33: 78 1953

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan
    • Russian Far East
      • Kuril Islands
      • Primorye
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000504235
Cornell Woody Plants 417
USDA Plants SKJA
Tropicos 28101410
INPN 123984
KEW urn:lsid:ipni.org:names:775237-1
The Plant List kew-2600234
Missouri Botanical Garden 286767
PFAF Skimmia japonica
Open Tree Of Life 790015
Observations.org 195715
NCBI Taxonomy 210365
NBN Atlas NBNSYS0200003186
IPNI 775237-1
iNaturalist 128909
iNaturalist 128912
iNaturalist 128910
GBIF 7269601
Freebase /m/043qfzl
EPPO SKMJA
EOL 5625406
Elurikkus 618122
USDA GRIN 34484
Wikipedia Skimmia_japonica
CMAUP NPO25008

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Temporal variation of allergenic potential in urban parks during the vegetation period: a case study from Bratislava, Slovakia Zahradníková E, Rendeková A, Ščevková J Environ Sci Pollut Res Int 05-Dec-2023
PMCID:PMC10791852
doi:10.1007/s11356-023-31137-9
PMID:38052730
Touch, feel, heal. The use of hospital green spaces and landscape as sensory-therapeutic gardens: a case study in a university clinic Dinu Roman Szabo M, Dumitras A, Mircea DM, Doroftei D, Sestras P, Boscaiu M, Brzuszek RF, Sestras AF Front Psychol 24-Nov-2023
PMCID:PMC10705765
doi:10.3389/fpsyg.2023.1201030
PMID:38078228
Quantifying heterogeneity in ecohydrological partitioning in urban green spaces through the integration of empirical and modelling approaches Stevenson JL, Birkel C, Comte JC, Tetzlaff D, Marx C, Neill A, Maneta M, Boll J, Soulsby C Environ Monit Assess 15-Mar-2023
PMCID:PMC10014787
doi:10.1007/s10661-023-11055-6
PMID:36918498
Recent advances in chemistry and therapeutic potential of functionalized quinoline motifs – a review Ajani OO, Iyaye KT, Ademosun OT RSC Adv 24-Jun-2022
PMCID:PMC9231466
doi:10.1039/d2ra02896d
PMID:35873320
Oxypeucedanin: Chemotaxonomy, Isolation, and Bioactivities Mottaghipisheh J Plants (Basel) 30-Jul-2021
PMCID:PMC8401860
doi:10.3390/plants10081577
PMID:34451622
Using Genealogical Concordance and Coalescent-Based Species Delimitation to Assess Species Boundaries in the Diaporthe eres Complex Hilário S, Gonçalves MF, Alves A J Fungi (Basel) 25-Jun-2021
PMCID:PMC8307253
doi:10.3390/jof7070507
PMID:34202282
Diversity in Chemical Structures and Biological Properties of Plant Alkaloids Bhambhani S, Kondhare KR, Giri AP Molecules 03-Jun-2021
PMCID:PMC8199754
doi:10.3390/molecules26113374
PMID:34204857
Diversification and selection pattern of CYP6B genes in Japanese Papilio butterflies and their association with host plant spectra Sato A, Okamura Y, Murakami M PeerJ 22-Dec-2020
PMCID:PMC7761194
doi:10.7717/peerj.10625
PMID:33391886
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
Overwintered Drosophila suzukii Are the Main Source for Infestations of the First Fruit Crops of the Season Panel AD, Zeeman L, van der Sluis BJ, van Elk P, Pannebakker BA, Wertheim B, Helsen HH Insects 22-Oct-2018
PMCID:PMC6315960
doi:10.3390/insects9040145
PMID:30360355
Circular spectropolarimetric sensing of higher plant and algal chloroplast structural variations Patty CH, Ariese F, Buma WJ, ten Kate IL, van Spanning RJ, Snik F Photosynth Res 23-Aug-2018
PMCID:PMC6548066
doi:10.1007/s11120-018-0572-2
PMID:30141032
Über das Alkaloid von Skimmia repens, Nakai Y. Asahina, T. Ohta, M. Inubuse Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1881.50.12_1117
Phylogenetic relationships of Vepris (Rutaceae) inferred from chloroplast, nuclear, and morphological data Morton CM PLoS One 08-Mar-2017
PMCID:PMC5342198
doi:10.1371/journal.pone.0172708
PMID:28273098
Development of microsatellite markers for the clonal shrub Orixa japonica (Rutaceae) using 454 sequencing Tamaki I, Setsuko S, Sugai K, Yanagisawa N Appl Plant Sci 18-Oct-2016
PMCID:PMC5077282
doi:10.3732/apps.1600066
PMID:27785383
Non-crop plants used as hosts by Drosophila suzukii in Europe Kenis M, Tonina L, Eschen R, van der Sluis B, Sancassani M, Mori N, Haye T, Helsen H J Pest Sci (2004) 24-Mar-2016
PMCID:PMC5318492
doi:10.1007/s10340-016-0755-6
PMID:28275324

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(1S,2S,4S,5S,6S,7S,8S,9R,12R)-6-(hydroxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecane-4,5,7,8,12-pentol 162992540 Click to see CC1CC(C(C2(C13C(C(C(C2O)O)C(O3)(C)C)O)CO)O)O 318.36 unknown https://doi.org/10.1039/J39700000556
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)91150-6
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1039/J39700000556
https://doi.org/10.1016/S0031-9422(00)91150-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
11-Oxo-alpha-amyrin 69166285 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1R,2R,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,15,20-trioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icosan-13-yl] acetate 137706495 Click to see CC(=O)OC1CC(=O)OC(C2C1(C3CCC4(C(OC(=O)C5C4(C3(C(=O)C2)C)O5)C6=COC=C6)C)C)(C)C 514.60 unknown https://doi.org/10.2503/JJSHS.67.835
[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-15-[(2R,3S,5R)-5-[(2S)-3,3-dimethyloxiran-2-yl]-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 3-methylbutanoate 163078747 Click to see CC(C)CC(=O)OC1CCC2(C3CCC45CC4(C3(C(CC2C1(C)C)O)C)CCC5C6CC(OC6O)C7C(O7)(C)C)C 572.80 unknown https://doi.org/10.1246/BCSJ.61.3225
[(1S,2R,3R,5R,7R,10S,11R,14R,15S)-15-[(3S,5R)-5-[(2S)-3,3-dimethyloxiran-2-yl]-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 3-methylbutanoate 54758525 Click to see CC(C)CC(=O)OC1CCC2(C3CCC45CC4(C3(C(CC2C1(C)C)O)C)CCC5C6CC(OC6O)C7C(O7)(C)C)C 572.80 unknown https://doi.org/10.1246/BCSJ.61.3225
[15-[5-(3,3-Dimethyloxiran-2-yl)-2-hydroxyoxolan-3-yl]-3-hydroxy-2,6,6,10-tetramethyl-7-pentacyclo[12.3.1.01,14.02,11.05,10]octadecanyl] 3-methylbutanoate 14165901 Click to see CC(C)CC(=O)OC1CCC2(C3CCC45CC4(C3(C(CC2C1(C)C)O)C)CCC5C6CC(OC6O)C7C(O7)(C)C)C 572.80 unknown https://doi.org/10.1246/BCSJ.61.3225
CID 326240 326240 Click to see CC(=O)OC1CC(=O)OC(C2C1(C3CCC4(C(OC(=O)C5C4(C3(C(=O)C2)C)O5)C6=COC=C6)C)C)(C)C 514.60 unknown https://doi.org/10.2503/JJSHS.67.835
Deacetylnomilin 139082180 Click to see CC1(C2CC(=O)C3(C(C2(C(CC(=O)O1)O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 472.50 unknown https://doi.org/10.2503/JJSHS.67.835
Isoobacunoic acid 20055680 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 472.50 unknown https://doi.org/10.2503/JJSHS.67.835
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.2503/JJSHS.67.835
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1R,2R,4S,7S,8S,11R,12R,13S,16R)-7-(furan-3-yl)-13-hydroxy-1,8,12,13,15,15-hexamethyl-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecane-5,18-dione 101592373 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)(C)O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 444.50 unknown https://doi.org/10.2503/JJSHS.67.835
3-[(1R,2R,5R,6R,7R,10S,11S,14S)-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-3,13-dioxo-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecan-6-yl]-3-hydroxypropanoic acid 101601415 Click to see CC12CCC3C(C(CC(=O)C3(C14C(O4)C(=O)OC2C5=COC=C5)C)C(C)(C)O)(C)C(CC(=O)O)O 490.50 unknown https://doi.org/10.2503/JJSHS.67.835
Calamin 131752311 Click to see CC12CCC3C(C(C(=O)C(C3(C14C(O4)C(=O)OC2C5=COC=C5)C)O)C(C)(C)O)(C)C(CC(=O)OC)O 520.60 unknown https://doi.org/10.2503/JJSHS.67.835
Cyclocalamin 13857944 Click to see CC1(C2C(=O)C(C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)O)C 502.60 unknown https://doi.org/10.2503/JJSHS.67.835
Nomilinic acid 131751863 Click to see CC(=O)OC(CC(=O)O)C1(C2CCC3(C(OC(=O)C4C3(C2(C(=O)CC1C(C)(C)O)C)O4)C5=COC=C5)C)C 532.60 unknown https://doi.org/10.2503/JJSHS.67.835
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
methyl (3S)-3-[(1R,2S,6S,10S,11S,14S)-11-(furan-3-yl)-3-hydroxy-2,6,10-trimethyl-4,13-dioxo-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecan-6-yl]-3-hydroxypropanoate 131752313 Click to see CC12CCC3C(CC(=O)C(C3(C14C(O4)C(=O)OC2C5=COC=C5)C)O)(C)C(CC(=O)OC)O 462.50 unknown https://doi.org/10.2503/JJSHS.67.835
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1039/J39700000556
https://doi.org/10.1039/P19740002177
https://doi.org/10.1055/S-2006-962804
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1039/J39700000556
https://doi.org/10.1248/YAKUSHI1881.50.12_1117
https://doi.org/10.1039/P19740002177
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Eduline 622180 Click to see CN1C2=C(C=C(C=C2)OC)C(=O)C=C1C3=CC=CC=C3 265.31 unknown https://doi.org/10.1039/J39700000556
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 346340 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(92)80484-V
7-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 320361 Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 324.28 unknown https://doi.org/10.1016/0031-9422(92)80484-V
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(92)80484-V
Skimmin 99693 Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 324.28 unknown https://doi.org/10.1016/0031-9422(92)80484-V
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1055/S-2006-962141
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(2S)-9-hydroxy-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yloxy]oxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 102146519 Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O 600.60 unknown https://doi.org/10.1016/0031-9422(92)80484-V
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(2S)-9-hydroxy-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yloxy]oxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 102155846 Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC(=C(C(=C5)OC)O)OC)O)O)O 630.60 unknown https://doi.org/10.1016/0031-9422(92)80484-V
[3,4,5-Trihydroxy-6-[2-(9-hydroxy-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl)propan-2-yloxy]oxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162870132 Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O 600.60 unknown https://doi.org/10.1016/0031-9422(92)80484-V
[3,4,5-Trihydroxy-6-[2-(9-hydroxy-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl)propan-2-yloxy]oxan-2-yl]methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 162885909 Click to see CC(C)(C1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC(=C(C(=C5)OC)O)OC)O)O)O 630.60 unknown https://doi.org/10.1016/0031-9422(92)80484-V
4-(2,3-Dihydroxy-3-Methylbutoxy)Furo(3,2-G)Chromen-7-One 483513 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown https://doi.org/10.1055/S-2006-962141
4-[(3,3-Dimethyloxiran-2-yl)methoxy]furo[3,2-g]chromen-7-one 160544 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1055/S-2006-962141
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1055/S-2006-962141
Oxypeucedanin hydrate 17536 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)O 304.29 unknown https://doi.org/10.1055/S-2006-962141
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1055/S-2006-962141
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1055/S-2006-962141
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1055/S-2006-962141
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1055/S-2006-962141
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1055/S-2006-962141

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